| Product NDC: | 68387-450 |
| Proprietary Name: | Silver Sulfadiazine |
| Non Proprietary Name: | Silver Sulfadiazine |
| Active Ingredient(s): | 10 mg/g & nbsp; Silver Sulfadiazine |
| Administration Route(s): | TOPICAL |
| Dosage Form(s): | CREAM |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 68387-450 |
| Labeler Name: | Keltman Pharmaceuticals Inc. |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | ANDA018578 |
| Marketing Category: | ANDA |
| Start Marketing Date: | 20070310 |
| Package NDC: | 68387-450-01 |
| Package Description: | 50 g in 1 JAR (68387-450-01) |
| NDC Code | 68387-450-01 |
| Proprietary Name | Silver Sulfadiazine |
| Package Description | 50 g in 1 JAR (68387-450-01) |
| Product NDC | 68387-450 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Silver Sulfadiazine |
| Dosage Form Name | CREAM |
| Route Name | TOPICAL |
| Start Marketing Date | 20070310 |
| Marketing Category Name | ANDA |
| Labeler Name | Keltman Pharmaceuticals Inc. |
| Substance Name | SILVER SULFADIAZINE |
| Strength Number | 10 |
| Strength Unit | mg/g |
| Pharmaceutical Classes | Sulfonamide Antibacterial [EPC],Sulfonamides [Chemical/Ingredient] |